Remote UK Study Start-Up Specialist – Clinical Trials in London

Remote UK Study Start-Up Specialist – Clinical Trials in London

London Full-Time 31500 - 38500 Β£ / year (est.) Remote
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At a Glance

  • Tasks: Manage activation tasks for UK clinical trial sites while working remotely.
  • Company: Join IQVIA, a leader in clinical research and innovation.
  • Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
  • Other info: Be part of a dynamic team shaping the future of healthcare.
  • Why this job: Make a difference in clinical trials and contribute to groundbreaking research.
  • Qualifications: 3 years in clinical research and a background in life sciences required.

The predicted salary is between 31500 - 38500 Β£ per year.

IQVIA is seeking a Country-level Site Activation professional to manage activation tasks for UK sites, working remotely with the SAM and project team. You will ensure regulatory readiness, maintain study documents, and monitor timelines in line with SOPs and ICH/GCP guidelines.

A background in life sciences and 3 years in clinical research are required. This home-based role requires strong knowledge of the UK clinical trial landscape and experience with regulatory submissions and ethics approvals.

Remote UK Study Start-Up Specialist – Clinical Trials in London employer: IQVIA

At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.

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Contact Details:

IQVIA Recruitment Team

We think you need these skills to ace Remote UK Study Start-Up Specialist – Clinical Trials in London

Regulatory Knowledge
Clinical Research Experience
Study Document Management
Timeline Monitoring
SOP Compliance
ICH/GCP Guidelines Familiarity
UK Clinical Trial Landscape Knowledge